drugset / Trial / NCT01745965

A Prospective, Randomized Multicenter, Open-label Comparison of Preoperative Trastuzumab Emtansine (T-DM1) With or Without Standard Endocrine Therapy vs. Trastuzumab With Standard Endocrine Therapy Given for Twelve Weeks in Patients With Operable HER2+/HR+ Breast Cancer Within the ADAPT Protocol.

NCT01745965

Phase 2 Completed 380 enrolled West German Study Group Roche Pharma AG · collab
RandomizedParallel-groupOpen-labelTreatment

Summary

Trial to optimize neoadjuvant therapy for HER overexpression and co-expressing of hormone receptors(ER and/or PR) breast cancer (HEr2+/HR+). A new high potential trastuzumab conjugate T-DM1(trastuzumab was linked with the cytotoxic agent mertansine DM1)was tested with endocrine therapy and without against a standard arm with trastuzumab and endocrine therapy.

Timeline

Start
2012-11
Primary completion
2015-02
Completion
2025-01-15

Drugs

EvaluationDrugModalityDoseRoute
Comparator Trastuzumab Monoclonal antibody 6 mg/kg
Subject Trastuzumab emtansine Other / unclassified 3.6 mg/kg

Indications